Outcomes and Patient Satisfaction After Colpocleisis for Pelvic Organ Prolapse

Completed

• Conditions: Pelvic Organ Prolapse
• Interventions: Other: Questionnaires, Physical Examination

• Registration Number: NCT00714155
• Lead Sponsor: University of Rochester

Brief Summary

The purpose of this study is to evaluate the long-term success rate of the colpocleisis procedure and its effect on quality of life in women who have this surgery. We want to see if women who have this surgery have problems with recurrent pelvic organ prolapse, urinary incontinence, or bowel problems after the surgery. We also want to see how the surgery affects women's sexuality.

Detailed Description

Not available

Study Timeline

• Study Start: 2006-07
• Study First Submitted: 2008-07-08
• Study First Submitted QC: 2008-07-11
• Study First Posted: 2008-07-14
• Primary Completion: 2009-01
• Study Completion: 2009-01
• Status Verified: 2011-11
• Last Update Submitted: 2012-06-13
• Last Update Posted: 2012-06-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 48

Inclusion Criteria

• women who underwent either total colpectomy with colpocleisis or partial colpectomy with LeFort-type colpocleisis performed by the Urogynecology service between 1/2000 and 12/2007 at Strong Memorial Hospital

Exclusion Criteria

• women who are not undergone colpocleisis or colpectomy

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
1	Questionnaires, Physical Examination	Physical examination, questionnaires, retrospective chart review
2	Questionnaires, Physical Examination	Questionnaires, retrospective chart review

Primary Outcome Measures

Name	Time	Method
Questionnaires	Post-operative

Secondary Outcome Measures

Name	Time	Method
Physical Examination	Post-operative

Trial Locations

Locations (1)

University of Rochester; 🇺🇸 Rochester, New York, United States